Self-limiting chemical vapor deposition and atomic layer deposition methods

ABSTRACT

Methods for depositing silicon on a semiconductor or metallic surface include cycling dosing of silane and chlorosilane precursors at a temperature between 50° C. and 300° C., and continuing cycling between three and twenty three cycles until the deposition self-limits via termination of surface sites with Si—H groups. Methods of layer formation include depositing a chlorosilane onto a substrate to form a first layer, wherein the substrate is selected from the group consisting of In x Ga 1-x As, In x Ga 1-x Sb, In x Ga 1-x N, SiGe, and Ge, wherein X is between 0.1 and 0.99. The methods may include pulsing a silane to form a silicon monolayer and cycling dosing of the chlorosilane and the silane. Layered compositions include a first layer selected from the group consisting of In x Ga 1-x As, In x Ga 1-x Sb, In x Ga 1-x N, SiGe, and Ge, wherein X is between 0.1 and 0.99, and a second layer, wherein the second layer comprises Si—H and Si—OH.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims benefit of U.S. Provisional Patent Application Ser. No. 61/912,930, filed Dec. 6, 2013, which is herein incorporated by reference in its entirety.

FIELD

Embodiments of the present disclosure generally relate to deposition of materials. Another field of the present disclosure is semi-conductor device fabrication technology. Particular applications of the present disclosure include the formation of silicon layers.

BACKGROUND

A sub 400° C. ALD process for growing monolayers of Si on clean surfaces by alternating pulses of Si₂H₆ and SiCl₄ employed with the substrate temperature varied between 355°-385° C. The process is slow, with each ALD cycle taking several minutes and the desorption of the HCl(g) biproduct being slow below 400° C. Other processes include monolayer silicon ALD growth on Ge with use of alternating pulses of Si₂Cl₆ and atomic hydrogen, or Si₂Cl₆ and Si₂H₆, at undesirably high substrate temperatures of 400°-465° C.

Physical vapor deposition (PVD) of silicon for passivation of III-V surfaces has been reported, but requires a silicon multilayer as the silicon is not ordered. Also, the PVD deposition of silicon is not compatible with processing of three dimensional devices such as finFETs on large semiconductor wafers.

SUMMARY

In one embodiment, a method for depositing silicon on a semiconductor or metallic surface comprises cycling dosing of silane and chlorosilane precursors at a temperature between 50° C. and 300° C. and continuing cycling between three and twenty three cycles until the deposition self-limits via termination of surface sites with Si—H groups.

In another embodiment, a method of layer formation comprises depositing a chlorosilane onto a substrate to form a first layer, wherein the substrate is selected from the group consisting of In_(x)Ga_(1-x)As, In_(x)Ga_(1-x)Sb, In_(x)Ga_(1-x)N, SiGe, and Ge, wherein X is between 0.1 and 0.99. The method may include pulsing a silane to form a silicon monolayer. The method may include cycling dosing of the chlorosilane and the silane.

In another embodiment, a layered composition comprises a first layer selected from the group consisting of In_(x)Ga_(1-x)As, In_(x)Ga_(1-x)Sb, In_(x)Ga_(1-x)N, SiGe, and Ge, wherein X is between 0.1 and 0.99, and a second layer, wherein the second layer comprises Si—H and Si—OH.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is overlaid XPS spectra illustrating the increase of the silicon 2p3/2 peak and the decrease in the gallium 3p3/2 peak according to some embodiments of the present disclosure.

FIG. 2 is overlaid XPS spectra illustrating the increase of the silicon 2p3/2 peak and the decrease in the gallium 3p3/2 peak according to some embodiments of the present disclosure.

DETAILED DESCRIPTION

In one embodiment, a method for depositing silicon on a semiconductor or metallic surface comprises cycling dosing of silane and chlorosilane precursors at a temperature between 50° C. and 300° C. and continuing cycling between three and twenty three cycles until the deposition self-limits via termination of surface sites with Si—H groups.

In another embodiment, a method of layer formation comprises depositing a chlorosilane onto a substrate to form a first layer, wherein the substrate is selected from the group consisting of In_(x)Ga_(1-x)As, In_(x)Ga_(1-x)Sb, In_(x)Ga_(1-x)N, SiGe, and Ge, wherein X is between 0.1 and 0.99. The method may include pulsing a silane to form a silicon monolayer. The method may include cycling dosing of the chlorosilane and the silane.

In another embodiment, a layered composition comprises a first layer selected from the group consisting of In_(x)Ga_(1-x)As, InGa_(1-x)Sb, In_(x)G_(1-x)N, SiGe, and Ge, wherein X is between 0.1 and 0.99, and a second layer, wherein the second layer comprises Si—H and Si—OH.

Embodiments of the present disclosure may provide self-limiting and saturating atomic layer deposition (ALD) and self-limiting and saturating chemical vapor deposition (CVD) of a silicon seed layer on a variety of non-silicon layer surfaces. Embodiments of the present disclosure may include depositing a silicon seed layer on substrates of varying ahoy compositions (e.g. indium gallium arsenide, indium gallium antiminide, indium gallium nitride, and silicon-germanium), as well as germanium and metallic substrates.

Embodiments of the present disclosure provide low temperature silicon ALD and can use different substrates. Embodiments provide a comparable drop in substrate temperature to 250° C. or less in addition to providing self-limiting and saturating ALD growth.

Artisans have failed, to the knowledge of the present inventors, to provide self-limiting and saturating silicon CVD on non-silicon surfaces despite studies and reports in the literature of temperature ranges at which hydrogen desorption occurs from similar applicable substrates of Si, Ge, and GaAs. The silane precursor self-limiting CVD process produces saturation when all surface sites are terminated by Si—H groups. Thus, desorption of H₂(g) from substrate surface sites may occur until all surface sites become terminated by Si—H. Increase of substrate temperature to 400° C. leads to continued ALD silicon growth on top of the self-limiting ALD silicon seed layer or on top of the saturated self-limited CVD silicon seed layer.

For oxide deposition, metal contact deposition, surface functionalization, surface passivation, and oxide nucleation, methods of the present disclosure provide advantages compared to typical current semiconductor and metal substrate surface preparation and controlled growth methods.

Methods of the present disclosure may provide for improved semiconductor and metal substrate surface preparation and controlled growth methods. Functionalization creates a surface that is reactive to ALD precursors. Passivation forms a monolayer that leaves the Fermi level unpinned. The monolayer nucleation is the initial layer of ALD deposition. The process is low temperature. In one embodiment, preparation, functionalization, passivation and ALD deposition is performed at 250° C. Certain surfaces and substrates will permit lower temperatures. Substrates that recombinatively desorb H₂ at lower temperatures, e.g., 150° C., permit use of lower temperatures. Examples include InGaAs and InAs.

Present silicon saturating and self-limiting ALD and CVD processes of the present disclosure achieve functionalization, passivation and monolayer nucleation at 250° C. (and lower for some substrates), which is much lower temperature, on both metallic and semiconductor substrates, than comparable silicon ALD procedures reported in literature. The self-limiting and saturating silicon CVD process at 250° C. is advantageous from a device fabrication standpoint compared to existing silicon ALD processes that are at significantly higher temperature (above 350° C.) and provide for continuous growth of silicon on silicon and is not self-limiting. A unique strong bonding of silicon to all crystal faces of In_(x)Ga_(1-x)As, In_(x)Ga_(1-x)Sb, In_(x)Ga_(1-x)N, SiGe, and Ge should enable transfer of the dangling bonds from the substrate to silicon, and silicon is readily hydrogen passivated even by molecular H₂ due to the uniquely strong Si—H bonds. The monolayer of —OH may be ideal for nucleating almost any metal ALD precursor.

The ability to passivate metallic surfaces provides additional applications beyond semiconductor device fabrication. For example, methods of the present disclosure can provide a surface protection against oxidation on metallic surfaces.

The present disclosure provides, for example, self-limiting and saturating atomic layer deposition (ALD) and self-limiting and saturating chemical vapor deposition (CVD) of a silicon seed layer on indium gallium arsenide (InGaAs), indium gallium antiminide (InGaSb), indium gallium nitride (InGaN), and silicon-germanium (SiGe) substrates of varying alloy compositions, as well as germanium and metallic substrates. Embodiments of the present disclosure also provide a procedure for ALD silicon on top of the self-limiting ALD silicon seed layer or on top of the saturated self-limited CVD silicon seed layer for continued growth of silicon.

A silicon monolayer deposited as described herein can serve several purposes. (1) The dangling bonds of the substrate will be transferred to silicon, which are then passivated by hydrogen, leaving the surface electrically passivated. (2) The saturated monolayer of silicon with H passivation will serve to protect the semiconductor or metallic substrate from oxidation. (3) The silicon monolayer with possible H termination (e.g. Si—H) can also be employed for deposition of gate oxide through functionalization by an oxidant such as HOOH(g), in order to create an Si—OH layer which would react with nearly any ALD precursor thereby eliminating the need for metal precursor nucleation (for example with trimethyl aluminum predosing) decreasing EOT and lowering border trap density and fixed charge associated with interfacial layers or even direct bonding of oxide to nonsilicon semiconductors. The same procedure can be used for other crystallographic faces such as In_(x)Ga_(1-x)As(110), In_(x)Ga_(1-x)Sb(110), In_(x)Ga_(1-x)N(110), SiGe(110), and Ge(110). Some ALD precursors such as those containing O or OH groups may directly react with the Si—H termination. (4) The silicon monolayer or silicon monolayer with additional oxide ALD can be employed for metal contact formation.

Experiments of the present disclosure will be understood by artisans in view of the general knowledge in the art and the description that follows to illustrate broader features of some embodiments of the present disclosure.

The experiments showed self-limiting ALD of silicon on semiconductor and metal surface. Dosing parameters for near saturation coverage of silicon on dean InGaAs surface through cyclic dosing of Si₂Cl₆ and Si₃H₈ were shown. Scanning Tunneling Microscopy (STM) and X-Ray Photoelectron Spectroscopy (XPS) measurements were performed to investigate surface bonding configurations and electronic structures of Si/InGaAs(001)-(2×4). Thermal annealing measurements were also performed during this time to demonstrate thermal stability of the surface.

The experiments also show self-limiting CVD of silicon on semiconductor and metal surfaces through dosing of Si₃H₈. Dosing parameters were determined for near saturation coverage of silicon on clean InGaAs surface. STM and XPS measurements were used to investigate surface bonding configurations and electronic structures of silicon/InGaAs(001)-(2×4). Thermal annealing measurements were also performed during this time to demonstrate thermal stability of the surface.

One embodiment includes a self-limiting atomic layer deposition procedure based upon the saturation of the substrate semiconductor or metallic surface sites through a surface termination with Si—H and Si—Cl groups by cyclic dosing of silane and chlorosilane precursors at 250° C. Silane precursors include: SiH₄, Si₂H₆, Si₃H₈, S₄H₁₀, Si₅H₁₂ and chlorosilane precursors include: SiCl₄, Si₂Cl₆, Si₃Cl₈. Once all surface sites are terminated with Si—H and Si—Cl groups, the reaction becomes self-terminating, as hydrogen and chlorine bond to silicon stronger than other semiconductor or metallic materials. The self-limiting and saturating chemical vapor deposition procedure is based upon the saturation of the substrate semiconductor or metallic surface sites through a surface termination with Si—H groups by dosing a silane precursor at 250° C. Once surface sites are terminated with Si—H groups, the reaction becomes self-terminating, as hydrogen bonds to silicon stronger than other semiconductor or metallic materials. Further silicon growth can occur on either the self-limiting atomic layer deposition or chemical vapor deposition saturated surfaces by raising the temperature to 400° C. The H₂(g) and HCl(g) desorption product occurs only slowly below this temperature at the point of surface saturation.

The self-limiting atomic layer deposition procedure in an experiment is discussed next. A decapped In_(0.53)Ga_(0.47)As(001)-(2×4) surface was dosed with 1 MegaLangmuir of Si₇Cl₆ followed by 1 MegaLangmuir of Si₃H₈ at a sample temperature of 250° C. This procedure constitutes one complete self-limiting and saturating ALD cycle. After three cycles, an X-ray photoelectron spectroscopy (XPS) spectrum is taken of the surface with a non-monochromatic aluminum channel X-ray flood source system at a glancing angle of 30° to produce surface sensitive spectra. The XPS spectra were also recorded following 13 and 23 total self-limiting and saturating ALD cycles. FIG. 1 shows the increase of the silicon 2p3/2 peak at 100 eV and the decrease in the gallium 3p3/2 peak at 105 eV, as indicated by the arrows for all three spectra as well as the spectra of the clean decapped surface for comparison.

As shown in FIG. 1: Non-monochromatic aluminum channel X-ray flood source system spectra for clean decapped In_(0.53) Ga_(0.47)As(001)-(2×4) surface (100), In_(0.53)Ga_(0.47)As(001)-(2×4) surface following 3 ALD cycles at 250° C. (102), In_(0.53)Ga_(0.47)As(001)-(2×4) surface following 13 ALD cycles at 250° C. (104), and In_(0.53)Ga_(0.47)As(001)-(2×4) surface following 23 ALD cycles 250° C. (106). The spectra are shown of the Ga 3p3/2 and Si 2p3/2 peaks. As shown in Table 1 and FIG. 1 (by, for example, the Ga 3p3/2 peak at 105 eV of 100, 102, 104 and 106) near saturation of silicon on In_(0.53)Ga_(0.47)As(001)-(2×4) surface is reached after 13 self-limiting ALD cycles at 250° C. Full saturation may involve about 50 pulses or a different operating temperature; since the kinetics are likely desorption limited there are a variety of puke times, desorption/purge times, and processing temperature which will suffice.

The raw counts corrected by Schofield photoionization cross sectional relative sensitivity factors are recorded for doublet peak pairs of As 2p, Ga 2p, In 3d, Si 2p, Cl 2p for the clean decapped In_(0.53)Ga_(0.47)As(001)-(2×4) surface (100) as well as the 3, 13, and 23 ALD cycle dosed surfaces at sample temperature 250° C. (102, 104 and 106, respectively) and are shown in Table 1.

TABLE 1 Non-monochromatic aluminum channel X-ray flood source system raw counts corrected by Schofield photoionization cross sectional relative sensitivity factors for clean decapped In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface (100), In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface following 3 ALD cycles at 250° C. (102), In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface following 13 ALD cycles at 250° C. (104), and In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface following 23 ALD cycles 250° C. (106). Surface As 2p Ga 2p In 3d Si 2p Cl 2p Clean decapped 184.8 155.2 689.9 0.0 0.0 In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface (100) 3 ALD cycles at 250° C. (102) 158.2 112.4 483.5 509.9 581.3 13 ALD cycles at 250° C. (104) 115.6 72.2 242.4 665.6 576.3 23 ALD cycles at 250° C. (106) 90.5 57.6 351.3 714.7 544.2

The raw counts corrected by Schofield photoionzation cross sectional relative sensitivity factors are recorded and listed in Table 2 as relative atomic ratios compared to the total As 3d peak. AH peaks ratios tabulated in Table 2 are from comparable low binding energies, including: Ga 3d, In 3d, Si 2p, Cl 2p, and Ta 4d total peak values for both doublet peak pairs, as well as the O 1s, C 1s peaks. Ratios are listed for the clean decapped In_(0.53)Ga_(0.47)As(001)-(2×4) surface (100) as well as the 3, 13, and 23 ALD cycle dosed surfaces at sample temperature 250° C. (102, 104 and 106, respectively). As shown in Table 2 and FIG. 1 (by, for example, the Ga 3p3/2 peak at 105 eV of 100, 102, 104 and 106) near saturation of silicon on In_(0.53)Ga_(0.47)As(001)-(2×4) surface is reached after 13 self-limiting ALD cycles at 250° C. Full saturation may involve about 50 pulses or a different operating temperature; since the kinetics are likely desorption limited there are a variety of pulse times, desorption/purge times, and processing temperature which will suffice.

TABLE 2 Non-monochromatic aluminum channel X-ray flood source system raw counts corrected by Schofieid photoionization cross sectional relative sensitivity factors and listed as relative atomic ratios compared to the total As 3d peak. All spin orbit split peaks include peak counts from both doublet pair peaks. Surface As 3d Ga 2p In 3d Si 2p Cl 2p O 1s C 1s Ta 4d Clean decapped 1.00 0.90 0.56 0.00 0.00 0.03 0.13 0.29 In_(0.53)Ga_(0.47)As(001)- (2 × 4) surface (100) 3 ALD cycles 1.00 0.78 0.37 0.39 0.44 0.32 0.38 0.35 at 250° C. (102) 13 ALD cycles 1.00 0.80 0.19 0.52 0.45 0.53 0.50 0.33 at 250° C. (104) 23 ALD cycles 1.00 0.81 0.30 0.62 0.47 0.51 0.62 0.34 at 250° C. (106) Ratio values are listed for clean decapped In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface (100), In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface following 3 ALD cycles at 250° C. (102), In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface following 13 ALD cycles at 250° C. (104), and In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface following 23 ALD cycles 250° C. (106).

The filled-state STM image may be obtained of In_(0.53)Ga_(0.47)As(001)-(2×4) surface following 23 self-limiting and saturating ALD cycles of 1 MegaLangmuir of Si₂Cl₆ followed by 1 MegaLangmuir of Si₃H₈ at a sample temperature of 250° C. as compared to the clean decapped In_(0.53)Ga_(0.47)As(001)-(2×4) surface. The dosed surface contains high atomic surface order and the surface should be terminated by Si—H, leaving the surface Fermi level unpinned.

The self-limiting and saturating CVD procedure may include a decapped In_(0.53)Ga_(0.47)As(001)-(2×4) surface dosed with 1 MegaLangmuir of Si₃H₈ at a sample temperature of 250° C. This procedure constitutes one complete self-limiting and saturating CVD cycle. After three cycles, an X-ray photoelectron spectroscopy (XPS) spectrum is taken of the surface with a non-monochromatic aluminum channel X-ray flood source system at a glancing angle of 30′ to produce surface sensitive spectra. The XPS spectra were also recorded following 13 total self-limiting and saturating CVD cycles. FIG. 2 shows the increase of the silicon 2p3/2 peak at 100 eV and the decrease in the gallium 3p3/2 peak at 105 eV, as indicated by the arrows for both spectra as well as the spectra of the clean decapped surface for comparison.

As shown in FIG. 2: Non-monochromatic aluminum channel X-ray flood source system spectra for clean decapped In_(0.53)Ga_(0.47)As(001)-(2×4) surface (200), In_(0.53)Ga_(0.47)As(001)-(2×4) surface following 3 CVD cycles at 250° C. (202), and In_(0.53)Ga_(0.47)As(001)-(2×4) surface following 13 CVD cycles at 250° C. (204). The spectra are shown of the Ga 3p3/2 peaks at 105 eV and Si 2p3/2 peaks at 100 eV.

The raw counts corrected by Schofield photoionization cross sectional relative sensitivity factors are recorded for doublet peak pairs of As 2p, Ga 2p, In 3d, Si 2p, Cl 2p for the clean decapped In_(0.53)Ga_(0.47)As(001)-(2×4) surface (200) as well as the 3 and 13 CVD cycle dosed surfaces at sample temperature 250° C. (202 and 204, respectively) and are shown in Table 3. The Ga 3p3/2 peak continues to diminish with 13 cycles (204) and near saturation of silicon on In_(0.53)Ga_(0.47)As(001)-(2×4) surface is reached after 13 self-limiting and saturating CVD cycles at 250° C. (204). H₂ desorption is close to zero at 250° C. on silicon.

TABLE 3 Non-monochromatic aluminum channel X-ray flood source system raw counts corrected by Schofield photoionization cross sectional relative sensitivity factors for clean decapped In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface (200), In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface following 3 CVD cycles at 250° C. (202), and In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface following 13 CVD cycles at 250° C. (204). Surface As 2p Ga 2p In 3d Si 2p Clean decapped 213.80 174.90 699.40 0.00 In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface (200) 3 ALD cycles at 250° C. (202) 130.10 119.40 545.40 320.10 13 ALD cycles at 250° C. (204) 111.50 97.10 472.40 603.10

The self-limiting and saturating CVD procedure includes a decapped In_(0.53)Ga_(0.47)As(001)-(2×4) surface dosed with 1 MegaLangmuir of Si₃H₈ at a sample temperature of 250° C. This procedure constitutes one complete self-limiting and saturating CVD cycle. After three cycles, an XPS spectrum is taken of the surface with a non-monochromatic aluminum channel X-ray flood source system at a glancing angle of 30° to produce surface sensitive spectra. The XPS spectra were also recorded following 13 total self-limiting and saturating CVD cycles. FIG. 2 shows the increase of the silicon 2p3/2 peak at 100 eV and the decrease in the gallium 3p3/2 peak at 105 eV, as indicated by the arrows for both spectra as well as the spectra of the clean decapped surface for comparison.

The raw counts corrected by Schofield photoionzation cross sectional relative sensitivity factors are recorded and listed in Table 4 as relative atomic ratios compared to the total As 3d peak. All peaks ratios tabulated in Table 4 are from comparable low binding energies, including: Ga 3d, In 3d, Si 2p, Cl 2p, and Ta 4d total peak values for both doublet peak pairs, as well as the O 1s, C 1s peaks. Ratios are listed for the clean decapped In_(0.53)Ga_(0.47)As(001)-(2×4) surface (200) as well as for the 3 and 13 self-limiting and saturating CVD cycle dosed surfaces at sample temperature 250° C. (202 and 204, respectively). As shown in Table 4 and FIG. 2 (by, for example, the Ga 3p3/2 peak at 105 eV of 200, 202, and 204) near saturation of silicon on In_(0.53)Ga_(0.47)As(001)-(2×4) surface is reached after 13 CVD cycles at 250° C. In some embodiments, longer doses of Si₃H₈ or 25+ cycles or a different operating temperature may be used; since the kinetics are likely desorption limited there are a variety of pulse times, desorption/purge times, and processing temperature which will suffice.

TABLE 4 Non-monochromatic aluminum channel X-ray flood source system raw counts corrected by Schofield photoionization cross sectional relative sensitivity factors and listed as relative atomic ratios compare to the total As 3d peak. All spin orbit split peaks include peak counts from both doublet pair peaks. Surface As 3d Ga 2p In 3d Si 2p Cl 2p O 1s C 1s Ta 4d Clean decapped 1.00 0.98 0.61 0.00 0.00 0.66 0.57 0.38 In_(0.53)Ga_(0.47)As(001)- (2 × 4) surface (200) 3 ALD cycles 1.00 1.01 0.53 0.31 0.00 0.10 0.37 0.38 at 250° C. (202) 13 ALD cycles 1.00 0.78 0.46 0.58 0.00 0.63 0.61 0.32 at 250° C. (204) Ratio values are listed for clean decapped In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface (200), In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface following 3 self-limiting and saturating CVD cycles at 250° C. (202), and In_(0.53)Ga_(0.47)As(001)-(2 × 4) surface following 13 self-limiting and saturating CVD cycles at 250° C. (204).

Many applications will be apparent to artisans from the above discussion. Particular applications include that the CVD or ALD deposited silicon monolayer is applicable for use as a semiconductor and metallic surface protection layer from unwanted oxidation. This application may serve useful during deposition and processing of gate stacks on FinFETs for MOSFETs. Embodiments of the present disclosure may provide surface termination by Si—H groups followed by functionalization with an oxidant, creating an Si—OH layer, which can be performed prior to oxide gate deposition and source drain contact formation. The same process can be used for a monolayer oxide on unpinning of source/drain contacts on MOSFETs which is critical for SiGe. The same process can be used in flash memory where thin high-k oxides are needed for low voltage operation.

While specific embodiments of the present disclosure have been shown and described, it should be understood that other modifications, substitutions and alternatives are apparent to one of ordinary skill in the art. Such modifications, substitutions and alternatives can be made without departing from the spirit and scope of the present disclosure, which should be determined from the appended claims.

Various features of the present disclosure are set forth in the appended claims. 

The invention claimed is:
 1. A method for depositing silicon on a semiconductor or metallic surface, the method comprising: cycling dosing of silane and chlorosilane precursors at a temperature between 50° C. and 300° C.; continuing cycling until the deposition self-limits via termination of surface sites with Si—H groups; and after self-termination, raising the temperature and depositing additional silicon.
 2. The method of claim 1, wherein the low temperature is at or below 250° C. and the surface is the surface of a substrate of one of In_(x)Ga_(1-x)As, In_(x)Ga_(1-x)Sb, In_(x)Ga_(1-x)N, SiGe, Ge and a metallic substrate.
 3. The method of claim 1, wherein the low temperature is at or below 150° C. and the surface is the surface of a substrate that recombinatively desorbs H₂ at or below 150° C.
 4. The method of claim 1, wherein the silane precursor is one of SiH₄, Si₂H₆, Si₃H₈, Si₄H₁₀, and Si₅H₁₂.
 5. The method of claim 1, wherein the chlorosilane precursor is one of SiCl₄, Si₂Cl₆, and Si₃Cl₈.
 6. A method of layer formation comprising: depositing a chlorosilane onto a substrate to form a first layer, wherein the substrate is selected from the group consisting of In_(x)Ga_(1-x)As, In_(x)Ga_(1-x)Sb, In_(x)Ga_(1-x)N, SiGe, and Ge, wherein X is between 0.1 and 0.99; pulsing a silane to form a silicon monolayer on the first layer; and cycling dosing of the chlorosilane and the silane.
 7. The method of claim 6, further comprising functionalizing the silicon monolayer with an oxidant.
 8. The method of claim 6, wherein the cycling dosing of the chlorosilane and the silane is performed within a range of 50° C. to 300° C.
 9. A layered composition, comprising: a first layer selected from the group consisting of In_(x)Ga_(1-x)As, In_(x)Ga_(1-x)Sb, In_(x)Ga_(1-x)N, SiGe, and Ge, wherein X is 0.53; and a second layer, wherein the second layer comprises Si—H and Si—OH.
 10. The method of claim 6, wherein the layer has a surface that recombinatively desorbs H₂ at or below 150° C.
 11. The method of claim 6, wherein the silane precursor is SiH₄, Si₂H₆, Si₃H₈, Si₄H₁₀, or Si₅H₁₂.
 12. The method of claim 6, wherein the chlorosilane precursor is SiCl₄, Si₂Cl₆, or Si₃Cl₈. 